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Kenny-Caffey syndrome

Disease Summary
Associated Targets (2)
Tbio

2


Explore Associated Targets
Mondo Description A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia.
Mondo Term and Equivalent IDs
MONDO:0016516:  Kenny-Caffey syndrome
DC:0000549: 
MESH:C537020: 
NCIT:C130991: 
OMIMPS:127000: 
Orphanet:2333: 
SCTID:82837002: 
UMLS:C0265291: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found